Conversion mechanisms of cobalt oxide anode for Li-ion battery: In situ X-ray absorption fine structure studies

被引:57
作者
Chae, Byung-Mok [1 ]
Oh, Eun-Suok [2 ]
Lee, Yong-Kul [1 ]
机构
[1] Dankook Univ, Lab Adv Catalysis Energy & Environm, Dept Chem Engn, Yongin 448701, South Korea
[2] Univ Ulsan, Sch Chem Engn, Ulsan 680749, South Korea
关键词
Anode; Cobalt oxide; In situ X-ray absorption fine structure; X-ray absorption near-edge structure; Direct conversion; ELECTROCHEMICAL PERFORMANCE; CO3O4; NANOPARTICLES; ELECTRODE MATERIALS; LITHIUM; CARBON; STORAGE; NANOCOMPOSITES; CAPACITY;
D O I
10.1016/j.jpowsour.2014.10.108
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Co3O4 powders as anode active materials for Li-ion battery are synthesized by a simple precipitation method. Physical properties of the prepared Co3O4 are characterized by N-2 physisorption, transmission electron microscopy, and X-ray diffraction. Conversion mechanisms upon the structural changes of Co3O4 anode are thoroughly studied by an in situ X-ray absorption fine structure (XAFS) technique. In the first cycle of discharge/charge, the X-ray absorption near-edge structure of Co reveals that the 1.1 V plateau of the discharging is ascribed to the direct conversion of Co3O4 to Co metal, and the 2.0 V plateau of the charging to the conversion of Co metal to CoO and Co3O4. In the second cycle of discharge/charge, the XAFS analysis reveals that a part of Co metal phase remains unconverted due to the phase isolation. It is demonstrated that the addition of a Conductive material can significantly improve the redox reaction of the Co3O4 anode material by minimizing the phase isolation. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:748 / 754
页数:7
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